ClinVar Miner

Submissions for variant NM_001903.5(CTNNA1):c.141C>G (p.Pro47=)

dbSNP: rs2149656171
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001459247 SCV001663085 likely benign not provided 2023-08-17 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005247101 SCV005896819 benign Hereditary diffuse gastric adenocarcinoma 2024-10-09 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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